SteriTite - The Container System of Choice

Case Medical provides a full range of disposables for use with its SteriTite, universal container. To order the appropriate consumables, review the information below.

SCS01:SteriTite Tamper-Evident Seals(1000 per case) Disposable plastic “pad” lock available in blue with chemical indicator dot for steamand EtO, and red for flash sterilization. White seals are recommended for hydrogen peroxide, STERRAD and V-Pro .SCF01:SteriTite Disposable Paper Filters(1000 per case) 100% Cellulose and water repellant. For steam sterilization. 7.5” round with posi-tioning hole.SCFM01:SteriTite Disposable Paper Filters(1000 per case) 100% Cellulose and water repellant. 10” X 4” Rectangular. For steam sterilizationSCF02:SteriTite Polypro Disposable Filters(1000 per case) Hydrophobic non-woven polypropylene, highly recomended for use for steam, gas,hydrogen peroxide and STERRAD sterilization.7.5”Round.SCFM02:SteriTite Polypro Disposable Filters(1000 per case) Hydrophobic non-woven polypropylene, highly recomended for use for use forsteam, gas, hydrogen peroxide and STERRAD sterilization. 10” X 4”Rectangular.SCL01:SteriTite Dual Process Indicator Cards(1000 per case) ID card with a dual chemical indicator. Use for steam and EO sterilizaton. SCL02:SteriTite Dual Indicator Cards, Small(1000 per case) ID card with a dual chemical indicator. Use with SC02,3,4M(G), SC02,3N(G) & tolock MediTray case trays. Use for steam and EO sterilization. SCI001:SteriTite Dual Process Indicators(1000 per case) A dual purpose indicator strip with room for process identification. Use for steam andEO sterilization. 8” Long with perforation may be reconfigure to two 4” long indicator strips. Place inopposing corners of inner tray.SCLH2023:SteriTite H2O2 Load Cards(1000 per case) ID card with chemical indicator. Use for STERRAD and V-Pro Sterilization.SCLH2024:SteriTite H2O2 Load Cards, Small(1000 per case) ID card with chemical indicator. Use for STERRAD and V-Pro Sterilization. Use with SC02,3,4M(G), SC02,3N(G), & to lock MediTray case trays.SCKIT1BP:SteriTite Disposable KitSteam and Gas Disposable Kit (Standard) 3 pk paper filters, 1pk seals, 1pk load cardSCKIT2BP:SteriTite Disposable KitSteam and Gas Disposable Kit (Mini/Narrow) 2 pk paper filters, 1pk seals, 1pk load cardSCKIT1WN:SteriTite Disposable KitH2O2 Disposable Kit (Standard) 3 pk Polypro filters, 1pk seals, 1pk load cardSCKIT2WN:SteriTite Disposable Kit H2O2 Disposable Kit (Mini/Narrow) 2 pk Polypro filters, 1pk seals,1pk load card.

Instructions for UseSteriTite®

If you have any questions regarding Case Medical products,please contact us at Phone: (201)-313-1999 Fax: (201) 373-9090

Info@casemed.com or www.casemed.com19 Empire Blvd, South Hackensack, NJ. 07606

Copyright 2010 Case Medical, Inc.®C

IFU Rev.S

THE MediTray® SYSTEM WARRANTY

Case Medical, Inc.®’s MediTray® product line is guaranteed to be free of functional defects in workmanship and materialswhen used as directed for its intended purpose. Case Medical, Inc.® will repair or replace, at their discretion, any MediTray® product found to have a manufacturing defect within three (3) years from the date of delivery at no charge to the customer.

THE SteriTite® SYSTEM WARRANTY

Case Medical, Inc.®’s SteriTite® product line is guaranteed to be free of functional defects in workmanship and materials when used as directed for its intended purpose. All SteriTite® products are warranted only to the originalpurchaser and only against defects in workmanship or materials which under the intended use render the product inoperable. Case Medical, Inc.®, at its sole option and without charge will either repair or replace any SteriTite®product determined to be defective in material or workmanship when used for its intended purpose.

Lid gasket and filter ring gaskets are under warranty for three (3) full years from the date of purchase.

The following exclusions apply to the MediTray® and SteriTite® product line replacement warranty: • Damage due to the use of caustic or abrasive cleaning agents. (Refer to Instructions for Use as to the proper specifications for the washing detergent. Case Medical recommends use of Case Solutions and SuperNova instrument cleaners or other pH neutral detergents).• Excessive handling abuse to the container bottom, container lid or filter cover ring and improper opening techniques.(Refer to Instructions for Use as to the proper latch opening techniques). • Damage from fire or other unpredictable event not under the control of Case Medical, Inc.®

CASE MEDICAL, INC.® RETURNED GOODS POLICY

Case Medical, Inc.® wants full customer satisfaction with its products, promptness, and customer service. Should youencounter a situation in which you wish to return a product, please contact our Customer Service Department at 1-888-227-CASE for proper authorization. All returns must be assigned an authorization number by Case Medical, Inc.® A completed Returned Goods Authorization (RGA) form must be affixed to the outside of all returned packages, showing prior cleaning and decontamination of returned merchandise. Issue of an RGAnumber should not be interpreted as a final credit to the customer account. Case Medical, Inc.® reserves the right toevaluate incoming returns prior to issuing any customer credit.

The following items are not returnable, except in the case of a manufacturing defect or product complaint:1. Products held longer than 60 days from the date of delivery.2. Products that have been used.3. Custom or modified products. 4. Discontinued products no longer carried on the current Case Medical Price List. 5. Products not properly packaged for returns.Non refundable products received by Case Medical will be returned directly to the customer with a letter of explanation.

Merchandise must be returned within 60 days from date of delivery. Product, which is not within the criteria of non-returnable merchandise, will be issued credit as follows:Credit will be issued for products returned in original packaging and resalable condition according to Terms and Conditions. Products returned after 30 days will be issued partial credit only.

SteriTite - The Container System of Choice

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Product Warranty

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The MediTray® System combines unbeatable protection of sensitive instrumentation with maximum convenience.Use the inserts for the MediTray® system and the SteriTite® sealed container system. MediTray® cases and coversmust be wrapped or placed in a sealed container for sterilization.

THE MediTray® SYSTEM WARRANTYCase Medical’s MediTray® product line is guaranteed to be free of functional defects in workmanship and materials when used as directed for its intended purpose. Case Medical, Inc.® will repair or replace, at their discretion, any MediTray® product found to have a manufacturing defect within three years from the date of

DEVICE DESCRIPTION: MediTray® is a rigid, reusable, medical sterilization packaging system validated forsteam and low temperature sterilization systems.

INTENDED USE: MediTray ® is intended to be used for the sterilization of reusable surgical instruments and medical devices in health care facilities. MediTray products may be containerized or wrapped with a FDA clearedmedical wrap. Please refer to the recommendations of your sterilizer manufacturer for specific reprocessing instructions as well as recommendations from your medical device manufacturer for material compatibility andrequirements for extended sterilization cycles. Note:MediTray products may be used in steam, EtO, ozone, V-Pro and H2O2 gas plasma (STERRAD) Sterilization. Caution: Nylon coated parts, color anodized parts and siliconemats are not recommended for STERRAD Sterilization.

REPROCESSING INSTRUCTIONSThoroughly clean and decontaminate MediTray® products prior to use. Use only pH neutral detergents. Abrasivecleaners, abrasive pads, or metal brushes cannot be used. MediTray® baskets and trays are recommended for automatic cleaning cycles. Be sure to follow all cleaning steps with a thorough rinse. Case Medical recommends itspH neutral Case Solutions and SuperNova cleaners for decontamination of medical devices including MediTray andSteriTite products. Dry product thoroughly before sterilization or further processing. A lint free cloth may be used forthe drying process.Warning: Use of a caustic cleaner can damage the anodized surface of aluminum devices and may cause corrosion. This practice will void the company’s warranty.

All MediTray® baskets, trays, and case-trays are designed with a unique patented grid pattern allowing for easy interchanging all inserts. BackBone® silicone brackets can be used to elevate and secure surgical instruments. For delicate instruments which require a firm yet cushioning grip, use BackBone® silicone brackets with patentedinner spine. BackBone® brackets have snap-in feet which attach securely to the base of your MediTray® basket,tray, or case-tray, without the need for tools. To remove a BackBone Bracket, push over with your fingers or palmto remove. If necessary, compress the snap-in feet on the underside with the MediTray® post tool or needle-nose pliers. MediTray metal brackets, partitions, and posts are secured with threaded nuts.

MediTray Labeling®

Manufacturer: Case Medical19 Empire Blvd, South Hackensack, NJ 07606Phone: (201) 313-1999 Fax: (201) 373-9090 www.casemed.com

If you have any questions regarding Case Medical products, contact us at info@casemed.com or call (201) 313-1999

delivery at no charge to the customer.

Authorized representative in Europe:Achim SchmitzAm Schilfrohr 147269 Duisburg, GermanyTel : 00491774483202Fax: 004932221323633Email: aschmitz@casemed.com

EC REP

The SteriTite sealed container and MediTray products are a universal, reusable packaging systemwith FDA 510k and CE mark for sterilization, transport and storage of medical devices includingflexible endoscopes according to manufacturer’s instructions. The SteriTite system has been validatedfor use in all current sterilization modalities, including prevacuum and gravity displacement steam,EtO, H2O2 sterilization including STERRAD 100, 100S, 200, NX, 100NX, AMSCO V-Pro 1, V-Pro 1Plus, V-Pro maX , as well as STERIZONE® 125L, and sealed immediate use steam sterilization

The SteriTite® rigid container system is available for both prevacuum and gravity displacement sterilizers. The perforated bottom containers can be used in both prevacuum and gravity displace-ment sterilizers, as well as, STERRAD and Steris V-Pro sterilization. Solid bottom containers can beused in pre-vacuum steam sterilization cycles only. The perforated bottom containers are ideal forstandardization as they are validated for all current sterilization methods.

MediTray baskets, trays and accessories are intended to organize, protect and secure devices duringsterilizaton, transport and storage. Case Medical has validated its MediTray products to be compati-ble with all sterilization modalities.

1 ANSI/AAMI ST79:2010/2011, ST77:2010 AAMI STANDARDS ORDER CODE: www.aami.org/publications/standards/index.html

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Whenever a new packaging method is introduced into a health care facility, all procedures associatedwith its use should be carefully evaluated and adapted. For this reason, Case Medical Inc. recommendsthat each user of our products become familiar with the information contained in “Comprehensiveguide to steam sterilization and sterility assurance in Health Care Facilities” and “Containment devices for reusable medical device sterilization”.1

SteriTite - The Container System of Choice®SteriTite Labelingfor Amsco V-PRO Low Temperature Sterilization System

®

DEVICE DESCRIPTION: The SteriTite® container is a rigid, reusable, sealed medical sterilization packaging system.INTENDED USE: The SteriTite universal container system with MediTray products is a reusable sterilization container system used to enclose other medical devices, which are to be sterilized, transported and stored by a healthcare provider. The SteriTite container system is intended for use in Steris Amsco V-Pro1,V-Pro1 Plus and V-Pro maX lowtemperature sterilization system. Please refer to the recommendations of the sterilizer manufacturer for specific pro-cessing instructions and to your medical device manufacturer for material compatibility.LOAD: The contents must be placed within an instrument basket or tray. Leave 1” of clearance in container. (for example a 3” high basket may be placed within a 4” high container). Case Medical validated maximum load of31.36lbs including container and contents. AAMI recommends a maximum of 25lbs total weight.

Note:All containers for Steris Amsco V-PRO low temperature Sterilization System are perforated bottom containers,which must be used with the single-use non-woven Polypro filter. All MediTray products excluding nylon coatedbrackets and silicone mats are compatible with V-Pro H2O2 sterilization.

PARAMETERS FOR USE:Use nonwoven polypropylene disposable filters: Disposable nonwoven Filter # SCF02 (7.5” diameter) and SCFM02(10”X4”) are a single use disposable medical device supplied nonsterile.In Non-lumen cycles, validation testing was performed with non lumened instruments including non-lumened rigidendoscopes and non-lumened hinged instruments like forceps or scissors.In Lumen cycles, validation testing was performed with blades and lumens. Only stainless steel lumened instru-ments of 3mm or larger and a length of 400mm or shorter for a maximum of 20 lumens per load should be processedIn Flexible cycle, validation testing was performed with single or dual lumen surgical flexible endoscopes in eitherof two load configurations (per sterilizer manufacturer instruction): a. Two flexible endoscopes and no additionalload, each having either a single lumen with a minimum inside diameter of 1mm and a maximum length of 1050mm:two lumens with one having an inside diameter of 1mm or larger and a length of 998mm or shorter and the secondone an inside diameter of 1mm or larger and a length of 850mm or shorter. b. One flexible endoscope and load, each having either: a single lumen with an inside diameter of 1mm or larger anda length of 1050mm or shorter two lumens with one having an inside diameter of 1mm or larger and a length of998mm or shorter and the second one an inside diameter of 1mm or larger and a length of 850mm or shorter. Adequate sterilant penetration and barrier properties were demonstrated using the SteriTite® rigid reusable containersystem and MediTray products in the Steris Amsco V-PRO low temperature Sterilization System under half cycle andfractional studies. Stackability of SteriTite® Containers in Steris Amsco V-PRO : MediTray baskets and trays may be stacked withinthe SteriTite container system as follows: up to two (2) instrument baskets or four (4) trays may be stacked. Caution: External stacking was not tested. Stacking SteriTite containers on top of each other in Steris Amsco V-PRO isnot recommended. Placement of SteriTite® Containers in V-PRO low temperature Sterilization System: Case Med-ical recommends that its containers be placed flat on the sterilizer shelf. All models of SteriTite containers can beplaced on each of the two shelves within the V-PRO low temperature Sterilization System. However, only one shelfcan be used to accommodate an 8" high perforated base SteriTite® container, because of height restrictions within thesterilizer’s chamber. MediTray Products including MediTray inserts, instrument baskets, stacking trays, BackBone sil-icone brackets, stainless and aluminum brackets, posts and partitions may be used in V-PRO Sterilization System.EVENT RELATED STERILITY MAINTENENCE: 30 days tested real time with daily handling events.Caution: In V-PRO sterilization use only compatible materials and instruments as stated in the V-PRO sterilizationsystem operating manual. Consult with your instrument manufacturer for the compatibility of various materials inV-PRO Sterilization System. Refer to V-PRO Sterilization System Operating Manual, instructions for use and labeling.

Validation testing was performed per AAMI ST79, TIR12, and EC Directive 93/42/EEC of 14 June1993 (Medical Devices Directive), CE Directions DIN 58952 and EN UNI 868 part 8.

The following instructions for use provide guidance for proper care, handling, and processing of medical devices when SteriTite containers and MediTray products are used.

The CE marking certifies that the product has met EU health, safety, and environmental.

Health care personal need to perform testing to verify the effectiveness of the container system in thehospital’s sterilizer. Place biological indicators/ integrators in opposing corners of each tray/basketwithin the container.

* CONTRAINDICATION- NOT KNOWN

Authorized representative in Europe:Achim SchmitzAm Schilfrohr 147269 Duisburg, GermanyTel : 00491774483202Fax: 004932221323633Email: aschmitz@casemed.com

EC REP

SteriTite Decontamination:

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® SteriTite Labelingfor Ozone Sterilization with disposable filter

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DEVICE DESCRIPTION: The SteriTite® container is a rigid, reusable, sealed medical sterilization packaging system.INTENDED USE: The SteriTite® container system is intended for use in 125L Ozone Sterilizer for sterilization ofreusable surgical instruments and medical devices in health care facilities. MediTray product may be containerized orwrapped with a FDA cleared medical wrap. Please refer to the recommendations of your sterilizer manufacturer forspecific processing instructions as well as recommendations from your medical device manufacturer for material compatibility.LOAD: The contents must be placed within an instrument basket or tray. Load may be distributed in layers usingMediTray baskets and trays. Leave 1” of clearance in container. Case Medical validated maximum load of 22lbsincluding container and contents. AAMI recommends a maximum of 25lbs total weight.

125L Ozone Sterilization: Use vented or solid base container for 125L Ozone sterilization. Use MediTray productsin the container to secure instrumentation. Recommended for sterilization of medical devices, including blades, andstainless steel lumened instruments of 3mm diameter or larger and a length up to 470 mm. Do not use silicone mats asit was not designed for this purpose. Slight discoloration with our device may occur in 125L Ozone sterilization.Cycle time: The sterilizer manufacturer determines 125L Ozone Sterilization cycle time. For example, the recomendedexposure time is 15 minutes. Cycle temperature: between 30.8°C and 36°C (87.4°F and 96.8°F).EVENT RELATED STERILITY MAINTENENCE DATA: SteriTite containers are event related and maintainsterility during transport and multiple handling events provided that the integrity of the seal is not broken. The associated sterility maintenance test consisted of challenging the perforated bottom SteriTite container with MediTrayproduct for 6 months real time with multiple handling events. Note: The user should contact their device manufacturerfor appropriate sterilization cycle conditions. (ANSI/AAMI ST 79:2006 – Comprehensive guide to steam sterilizationand sterility assurance in health care facilities). Use paper or nonwoven disposable filters: Disposable paper filter #SCF01, SCF02 (7.5” diameter) SCFM01 and SCFM02 (10”X4”) are disposable medical device supplied nonsterile.Stackability of SteriTite® Containers in 125L Ozone Sterilization: External Stacking: Up to three (3) containers can be stacked and processed in the 125L Ozone Sterilizer. InternalStacking: Testing was done with up to three (3) stacked trays or baskets inside the containers. Adequate sterilant penetration and barrier properties were demonstrated using the SteriTite® rigid reusable container system and MediTray products in the 125L Ozone Sterilization System under half cycle and fractional studies. Caution: In 125L Ozone process only lumened instruments of 3mm or larger and a length up to 470 mm. Caution: In 125L Ozone Sterilization use only compatible materials and instruments as stated in the Ozone 125L Operating Manual. Specifically: Consult with your instrument manufacturer as to the compatibility of various materials in Ozone 125L Sterilization. Refer to TSO3 125L Ozone System Operating Manual instructions for use andlabeling. MediTray Products including MediTray inserts, instrument baskets, stacking trays, BackBone silicone brackets, stainless and aluminum brackets, posts and partitions may be used in 125L Ozone Sterilization. Caution: Do not use nylon coated brackets or silicone mat in 125L .VALIDATION TESTING: Case Medical subscribes to the overkill principle. SteriTite and MediTray products arevalidated under fractional and half cycle conditions.

PARAMETER FOR USE:

1. Disassemble all components. Unlatch and remove the lid of the SteriTite® rigid container. Remove filter retention plates from lid and base by turning the handle of the locking mechanism clockwise. Do not remove the gasket for the cleaning procedure. Remove filters and all other disposables and discard.

2. Remove the tray of contaminated instruments and prepare the instruments for decontamination following the recommendations of the instrument manufacturer.

3. Clean your MediTray® and SteriTite® products after each use with a pH neutral/enzymatic detergent and a soft, lint free cloth. Do not use abrasive cleaners, abrasive pads, or metal brushes. MediTray® baskets and trays can also be cleaned in an automatic washer. When using an automated washer, place filter retention plates in an instrument basket for cleaning.

4. Remove all detergent residue with a thorough rinse. If visible moisture is present, dry with a lint free cloth.

5. Examine each component for cleanliness.

Cleaning and DecontaminationCase Medical recommends that containers are reprocessed as soon as possible following use. Excess soil should beremoved after use by rinsing or wiping the device prior to the cleaning procedure. Personal Protective Equipment(PPE) should be worn when handling or working with contaminated or potentially contaminted materials, devicesand equipment. PPE includes gown, mask, goggles or face shield, gloves and shoe covers. Thoroughly clean anddecontaminate MediTray® products prior to first use and after each use with contaminated instruments (prior tosterilization). Details of proper cleaning procedures are as follows:

The hospital is responsible for in-house procedures for the disassembly, reassembly, inspection and packaging ofinstrument sets including container systems after they are thoroughly cleaned in a manner that will assure sterilant penetration and adequate drying. Prior to using the SteriTite and MediTray for the first time follow thecleaning procedures in this IFU and perform a visual inspection of all parts.

Automated Cleaning:SteriTite containers may be cleaned in automated washers or cart wash-ers when pH neutral detergents or enzymatic cleaners are used. Alwaysfollow with a thorough rinse to remove detergent residue. Follow therecommended dosage of the detergent If an automatic washer is used,secure all parts to avoid excess movement during cleaning. Make surethe container latches are folded inward and the handles are tucked withinthe racks so they don’t protrude.

Manual Cleaning:SteriTite containers may be cleaned manually with a soft lint free clothand a pH neutral detergent. Always follow with a thorough rinse to re-move detergent residue. Use a soft lint free cloth to dry all componentsof the container. Try to avoid water collection by washing and dryingthe container upside-down.

Recommendation: Case Solutions or SuperNova multi-enzymaticcleaners are ideal for medical devices and sterilization containers. Inaddition, single use enzymatic towelettes such as Penta Wipes can beused to decontaminate container components and Alcohol Wipes facilitate drying.

Caution: Do not use alkaline detergents or scratch pads. Caustic detergents will oxidize the anodized aluminum surface of the containerand create discoloration and corrosion.

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DEVICE DESCRIPTION: The SteriTite® container is a rigid, reusable, sealed medical sterilization packaging system.INTENDED USE: The SteriTite® container system is intended to be used for the sterilization of reusable surgicalinstruments and medical devices in health care facilities. MediTray product may be containerized or wrapped with a FDA cleared medical wrap. Please refer to the recommendations of your sterilizer manufacturer for specific processing instructions as well as recommendations from your medical device manufacturer for material compatibilityLOAD: The contents must be placed within an instrument basket or tray. Load may be distributed in layers using MediTray basic trays. Leave 1” of clearance in container. Case Medical validated maximum load of 22lbsincluding container and contents. AAMI recommends a maximum of 25lbs total weight.

PARAMETERS FOR USE:EO Sterilization: SteriTite containers may be used in EO sterilization for sterilization of blades and lumens. Solidbottom containers may be used in EO pre-vacuum sterilizers. Residual analysis shows that EO and EC limits were found to be well below maximum limits after 12 hours post aeration at room temperature. Recommended exposure time in: 600 mg/liter EO gas mixture (90% CO2 / 10% EO) - 2 hours.

230 mg/liter EO gas mixture (91.5% CO2 / 8.5% EO) - 3 hours.Polymeric and porous materials may require extended EO exposure time. Items with lumens should be throughly dried for EO sterilization.In EO sterilization, metal lumened devices of 2.2mm diameter or larger and length up to 457 mm and porous lumeneddevices of 3mm diameter or larger and length up to 400 mm may be processed. Contact your medical device manufacturer for specific processing information. EVENT RELATED STERILITY MAINTENENCE DATA: SteriTite containers are event related. Maintains sterility during transport and multiple handling events provided that the integrity of the seal is not broken. The associated tests consisted of testing samples after 90 days (real time) handling events at a health care facility. The perforated SteriTite container with MediTray product was tested in an event related study with daily handlingevents over a 30 to 90 day period.WARNING: Prepare complex instruments according to the instrument maker’s instructions. Use of nonabsorbenttray liners can cause condensate to pool. Do not use peel pouches within sealed containers, as they cannot be placedon their side for sterilization.Stackability of SteriTite® Containers in EO sterilization: Up to three (3) SteriTite containers can be stacked andprocessed in the sterilizer.VALIDATION TESTING: Case Medical subscribes to the overkill principle. SteriTite and MediTray products arevalidated in independent laboratories under fractional and half cycle conditions.

SteriTite Labelingfor EO Sterilization using disposable filter

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1. Perform a visual inspection of all parts prior to each use. Check that gaskets are properly secured and free ofwear or damage. Latches should function properly. The case and lid should be free of dents that may interferewith the seal. The aluminium surface of the container should have no noticeable corrosion or damage. Be surefilter retention plates or valve plates fit securely.

2. Verify that gaskets in the lid and in the filter retention plate(s) are pliable, without cracks or tears, andthat they are all properly and firmly affixed. Note: Testing has been completed by Case Medical, Inc® that verified gasket function after 501 cycles inSTERRAD® 100NX® Sterilizer and 1000 cycles in steam sterilization.

3. The retention plate should be flat when placed on a solid surface and should not spin freely when engagedwith the positioning pin. If the retention plate is loose, adjust the tension by pressing downward along theperimeter of the round plate, and upward at the tabs located at the ends of the rectangular plate. Never deformretention plate by bending at center point.

4. Verify that the positioning pin in the lid and base, as well as the label holders on the front of the SteriTite®

Container are secure.

The recommended inspection criteria should be performed after each use, because of the variables associated with cleaning agents and equipment.

5. For SteriTite® Universal Containers with a perforated base, place the appropriate filter over the perforations on the lid and base of the SteriTite®

Container and place the filter retention plate over the filter. Secure the filterretention plate by pushing downwards at center point (where indicated) and rotate the handle counter-clockwise to close.Note: Paper filters should be used only for steam and EtO sterilization.

Non- woven Polypro filters must be used for H2O2 STERRAD and V-Pro sterilization.

6. Select the appropriate size basket(s) or tray(s) according to container size. Arrange the clean instruments in thebasket(s) according to hospital procedures. Review the recommendations provided by the device manufacturer.MediTray® partitions, brackets and posts are recommended for easy loading and unloading as well as protection ofyour delicate instruments. Place the prepared baskets into the base of the SteriTite® container. Note: Do not exceed the height of the basket when placing instruments into the basket.To determine containersize, add one (1) inch of clearance for proper fit of contents( approximately 1/2 inch from the lid and 1/2 inch fromthe base. Case Medical has validated its SteriTite container system for stacking multiple layers within the con-tainer. The use of absorbent liners are not recommended for usewith the SteriTite container.

7. Place a process indicator or integrator in the corner of the instrument basket.

Note: An internal process indicator should be used within each container. It should be placed in the area of thecontainer considered to be least accessible to sterilant penetration...the corners of the container and the under-side of the lid, away from the filters, are the likliest locations for air pockets.

Note: Rectangular filters should only be used for the rectangular filter retention plates. The round filters should be used for the round filter retention plates.

SteriTite Assembly for Use:

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DEVICE DESCRIPTION: The FlashTite valve plate(s) are attachments to the SteriTite rigid reusable sealed container for pre-vacuum flash and gravity displacement flash steam sterilization cycles.INTENDED USE: The SteriTite sealed container with FlashTite valve plate(s) is intended to be used for sterilizationof one instrument or instrument set in flash sterilization.NOTE: Flashed items are for immediate use only, per AAMI guidance. Product was tested for sterility maintenancefor 24 hour shelf life. The FlashTite valve is recommended for one (1) year of use or 400 cycles. Record date of firstuse for your records. Use MediTray basic trays for flash sterilization cycles. LOAD: The contents must be placed within an instrument basket or tray. FlashTite systems for gravity displacementsteam flash sterilization require a load restricting basket designed to clear the FlashTite valves placed on the lid andon the base.

PARAMETERS FOR USE:Pre-vacuum Immediate Use Sterilization: Use either vented or solid base container with the same number ofFlashTite valve plate(s) as the number of vents. Recommended parameters are 4 minutes exposure at 270°F (132°C).Recommended dry time for SteriTite container with FlashTite valve plate(s): 0- 3 minutes dry time in the autoclavefor items processed in flash sterilization depending on the degree of dryness required. Gravity Displacement IUSS Sterilization: Use only perforated bottom container. Attach FlashTite valve plate(s) over all vents. Recommendedparameters are a minimum of 5 minutes exposure for non-porous items at 270°F (132°C) and minimum of 10 min-utes exposure for porous items, lumens and mixed loads at 270°F (132° C). Recommended dry time: 0- 3 minutes drytime in the autoclave for items processed in flash sterilization depending on the degree of dryness required. Note: Donot use the FlashTite valve with SteriTite perforated bottom models SC04HG, SC04QG and SC04FG, because of heightrestrictions within these containers. Do not use solid bottom SteriTite container with FlashTite valve in gravity dis-placement IUSS sterilization. Important: Clean after each use with pH neutral detergent.Note: “The evaluation of the container/sterilizer combination is especially important in gravity displacement steamsterilization because of the relative inefficiency of air removal in this sterilization process. The user must review thedata upon which the container manufacturer bases the recommended cycle time and must verify those results in thehospital’s sterilizer.” ANSI/AAMI ST79: 2010/2011 . Caution:When abbreviated dry time is implemented, moistureis present. Use a glove or towel when transporting hot items from the autoclave. Do not mix the FlashTite valve plate(s) with the filter retention plate(s) and disposable filter(s). Do not use theFlashTite valve plate(s) for EO or gas plasma (STERRAD) sterilization. Reprocessing Instructions:After each use, disassemble and decontaminate the FlashTite valve plate with a multi-enzymatic, pH neutral detergent as youwould any SteriTite component part. Thoroughly rinse and dry. Case Medical recommends that: A chemical indicator or integrator should be placed in every container for process-ing. Within the sealed container, place indicator in opposing corners. Case Medical recommends use of the 3M rapidread out biological indicator for verification.Note: The copper module within the FlashTite valve mechanism will darken over time. This color change will notimpact the safety and effectiveness of the device. Refer to the sterilizer manufacturer’s “Instructions for Use”for specific information as to the limitations of instrumentation, specifications and material compatibility. Complex instruments should be prepared and sterilized according to the instrument manufacturer’s instructions. Contact the manufacturer of your endoscope or lumened devices when flashing.VALIDATION TESTING: Case Medical subscribes to the overkill principle. SteriTite and MediTray products arevalidated in independent laboratories under fractional and half cycle conditions.

Either perforated bottom or solid bottom SteriTite containers may be used with FlashTite valve plate in pre-vac-uum steam immediate use sterilization. Use MediTray basic trays for flash sterilization cycles. The SteriTite solidbottom containers including 4” high models may be used for flash sterilization with FlashTite valve plate(s) in lid.

SteriTite Labeling®

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SteriTite Assembly for Use:®

for Immediate Use Sterilization using FlashTite valve plate(s)

8. Place the lid on top of the base. The edge of the base will fit in the lid channel creating a knife edge fit.

9. Place the lid on top of the base. The edge of the base will fit in the lid channel creating a knife edge fit.

10. Place the appropriate metal ID tags in the label holders located oneither side of the container latches. The label holder on the right canaccomodate a load card available from Case Medical, Inc®. Only clearID tags can be used in H2O2 sterilization.

11. Thread the guide on the SteriTite® tamper- evident seal through the lock holder and secure. Repeat on both latches. Blue and red tamper evident seals are available for steam and gas. White tamper evident seals are recommended for H2O2/ STERRAD Sterilization.

Caution: Use of any non-approved tamper evident seal could damagethe locking clip.

Place the SteriTite® Container flat on the shelf of the sterilizer cart. If needed, up to three (3) containers may be stacked and processed in an autoclave. If sterilized in a mix load, place containers below wrappedor linen items.

12. Consult the recommendations of your sterilizer manufactuer to determine the correct parameters regarding temperature, weight load, drytime,instrument processing and pre- and post-conditioning cycles.

Note: To minimize the potential of condensate formation in containers,crack the door of the autoclave for 15mins. Caution: Use of the SteriTite container in gravity displacement steam may increase exposure time for 15 mins. Then remove for cool down.

An external indicator or load card should be attached to the container at thistime. Case Medical provides external indicators for steam and EtO as well asH2O2 (STERRAD and V-Pro) sterilization.

13. Following the steam sterilization process, the cart should be removed from the autoclave and placed incool down. For low temperature sterilization modalities remove the container from the sterilizer and place inthe storage area.

Note: The SteriTite container with paper filter may be used for immediate use pre-vacuum steam sterilization cycles.

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SteriTite At Point of Use:®SteriTite Labeling®

for STERRAD Sterilization using disposable PolyPro filter

DEVICE DESCRIPTION: The SteriTite® container is a rigid, reusable, sealed medical sterilization packaging system. INTENDED USE: The SteriTite® container system is intended for use in STERRAD 100, 100S, 200, STERRADNX and 100NX sterilizers for the sterilization of reusable surgical instruments (blades and lumens) and for medicaldevices in health care facilities. MediTray products may be containerized or wrapped with a FDA cleared medicalwrap. Please refer to the recommendations of your sterilizer manufacturer for specific processing instructions and toyour medical device manufacturer for material compatibility.LOAD: The contents must be placed within an instrument basket or tray. Leave one (1)inch of clearance in con-tainer. Case Medical validated maximum load of 31.95 lbs including container and contents. AAMI recommendsa maximum of 25lbs total weight. For STERRAD 100,100S, 200, NX and 100NX use only perforated base SteriTite®containers with polypropylene filter. .

Use nonwoven polypropylene disposable filters: PolyPro filter # SCF02 (7.5” diameter) and SCFM02 (10”X4”) a medical device supplied nonsterile. In STERRAD 100, 100S & 200 process only stainless steel lumened instruments of3mm diameter or larger and a length up to 400 mm. In STERRAD NX standard cycle, process stainless steel lumenedinstruments of 2mm diameter or larger and up to 400 mm in length. In STERRAD NX advanced cycle, process stainless steel lumened instruments of 1mm diameter or larger and up to 500 mm in length and porous lumens (flexibleendoscope) of 1mm diameter or larger and up to 850 mm in length. In the STERRAD 100NX Standard cycle,process stainless steel lumened instruments of 0.7mm diameter or larger and up to 500mm in length. In STERRAD 100NX Flexible cycle, process flexible endoscopes, PE/PTFE lumened instruments of > 1.2mm x <835 mm.STERRAD Systems have pre programmed cycles for each unit. Cycle time: The sterilizer manufacturer determines STERRAD® Sterilization cycle time. Caution: In STERRAD® Sterilization do not use materials made of cellulose (paper filters and cotton) with SteriTite®containers. Caution: In STERRAD® Sterilization use only compatible materials and instruments as stated in theSTERRAD® Operating Manual. Consult with your instrument manufacturer as to the compatibility of various materi-als in STERRAD® Sterilization. Refer to ASP’s STERRAD® System Operating Manual, instructions for use and la-beling. Internal Stacking: MediTray baskets and trays may be stacked within the SteriTite container system asfollows: In STERRAD NX up to two (2) instrument baskets or trays may be stacked within the SteriTite container. Inthe STERRAD 200 up to four (4) instrument baskets or trays may be stacked. In STERRAD 200 & NX, the followingMediTray baskets are not intended to be stacked : BSKF04, BSKF06, BSKH04, BSKQ04, and BSKQ06. In addition,MediTray insert boxes are not intended to be stacked. Case Medical recommends that its containers be placed on thesterilizer shelf. External stacking was not tested. For STERRAD 100, 100S, 200 & 100NX : All models of SteriTitecontainers, can be placed on each of the two shelves within the STERRAD® 200. However, only one shelf can beused to accommodate an 8" high perforated base SteriTite®container, because of height restrictions within the sterilizer’s chamber. For STERRAD NX only 2",3” and 4" high containers will fit in the sterilizer chamber. EVENT RELATED STERILITY MAINTENENCE DATA: 120 days tested in real time (not extrapolated) w/ dailyhandling events.MediTray Products including MediTray inserts, instrument baskets, stacking trays, BackBone silicone brackets, stain-less and aluminum brackets, posts and partitions may be used in STERRAD Sterilization, wrapped or containerized. Caution: Do not use nylon coated brackets or silicone mat.VALIDATION TESTING: Adequate sterilant penetrationand barrier properties were demonstrated using the SteriTite® rigid reusable container system and MediTray®products in the STERRAD® Sterilization Systems (100S, 200, NX®, and 100NX®) under half cycle and fractional studies. STERRAD® Systems have preprogrammed cycles for each unit.

Note: For STERRAD 100, 100S, 200, 100NX all models of SteriTite perforated bottom sealed containers may be used except for the SC05WG, SC04LG and SC06LG which does not fit the STERRAD chamber. For STERRAD NX Sterilization only the SC02MG,SC03MG,SC04MG,SC02NG,SC03NG,SC04HG,SC04QG and SC04FG containers can be used due to STERRAD NX size.

9

4. Remove the lid, using the rings on the top of the lid to avoid contaminating the contents of the container.

1. Before opening the SteriTite® Container always verify that:The tamper-evident seals are intact.The disposable filter is visible through the perforations.The acceptability of the end point response of the external chemical indicator or load card. The correct set has been selected.

2. Break open the tamper evident seals, remove and discard.

3. Unlatch the container by pulling upward to release.The latches will fall away from the container edge toavoid recontamination of contents.

5. The scrub person should check the end point responseof the chemical indicator to verify acceptable results.

7. At the completion of the procedure, the SteriTite®Container can be used to contain and transport con-taminated instruments to the decontamination area.

Caution: Case Medical recommends that SteriTite®

Containers sterilized in an outside contract facitliyshould be double wrapped in plastic bags duringtransport.

The SteriTite container system and MediTray products are universal reusable packaging systems for medical devices to beused for sterilization including STERRAD 100S, 200, NX,100 NX, steam, EtO, Sterizone and V-Pro sterilization.

A SteriTite containment system with a solid lid and solid baseis available for soaking and transporting contaminated instruments to the decontamination area.

6. The scrub person will then remove the basket or baskets of instruments in a straight upward position and then place in the sterile field. Note:MediTray baskets and inserts are designedfor aseptic removal of contents.

Sterilitiy Maintenance Procedures

Ensure that a filter has covered all perforation in •lid and or base.Check that filter retention plate is securely •placed over filter.Gasket should be engaged in its lid channel.•Container edge is free of dents or damage.•Check that the internal and external chemical •indicator is present per hospital protocol.Check that there is no residual moisture in the•container.

Endpoint color change: The SteriTite container provides a location in the label holder for a chemicalprocess indicator card to differentiate a processedfrom unprocessed load. For steam and EtO steriliza-tion, the tamper evident seal contains a process indi-cator. In steam sterilization, the color change is fromcream to brown and in EtO cream to orange. InSTERRAD Sterilization, the color change on the loadcard is red to orange/yellow.

PARAMETERS FOR USE:

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SteriTite Labeling®

Reprocessing Instructions and Inspection Criteria

DEVICE DESCRIPTION: The SteriTite® container is a rigid, reusable, sealed medical sterilization packaging system. INTENDED USE: The SteriTite® container system is intended to be used for the sterilization of reusable surgicalinstruments and medical devices in health care facilities. MediTray products may be containerized or wrappedwith a FDA cleared medical wrap. Please refer to the recommendations of your sterilizer manufacturer for specificreprocessing instructions as well as recommendations from your medical device manufacturer for material compatibility and requirements for extended sterilization cycles.

REPROCESSING INSTRUCTIONS AND INSPECTION CRITERIA:1. Clean after each use. Disassemble all container components. Clean manually using a soft, lint free cloth orprocess in an automated washer. If an automated washer is used, secure parts to avoid excess movement duringprocessing. Make sure container latches are folded inward and handles are tucked within the racks and not protruding. The filter retention plate should be removed and placed in a basket for the cleaning process.2. Always use a pH neutral detergent, recommended for use on aluminum. Multi-enzymatic cleaners may be usedif they are pH neutral. Caution! Do not use abrasive cleaners, alkaline or acidic detergents, metal brushes or abrasive pads. 3. Rinse all components to prevent detergent residue. Dry thoroughly.4. Do a visual inspection of all parts. Check that gaskets are properly secured and free of wear or damage. Latchesshould function properly. Case and lid should be free of dents, which may interfere with the seal. Be sure filter retention plate or valve plate fits securely. 5. Verify the integrity of gaskets and other component parts. 6. Remove the filter retention plate(s) by turning the handle of the locking mechanism clockwise. Adjust filter retention plate by bending down along the edge to modify the tension.7. Replace the disposable filter after each use.8. Secure the filter by turning handle counter clockwise.9. Load the container with DRY surgical instruments.10. Place chemical indicators or integrators on each level of surgical instrument tray. For SteriTite® sealed containers place chemical indicators, integrators or biological indicators in corners of the basket or tray within thesealed container.11. Secure the container by latching the lid to the base. The top of the latch fits over the ridge in the lid of the container. Push bottom section of the latch over the lock hold (clip). Thread a disposable tamper evident sealthrough the latching mechanism.12. Place the proper load cards with complete information in the label holder on the right side of container latches.13. If the containers are sterilized in an outside contract facility, they should be doubled wrapped in double plasticbags during transport.14. Check with your sterilizer manufacturer for additional information on reprocessing sterilization containers intheir sterilizer.

Recommendations:Always use a pH neutral detergent for cleaning anodized aluminum sterilization containersand trays. Case Medical highly recommends its validated pH neutral Case Solutions and SuperNova instrumentcleaners for decontamination of the SteriTite container system and other sealed container systems.Warning: Use of a caustic cleaner will damage the anodized surface of aluminum devices and can cause corrosion. This practice will void the company’s warranty on its container system. Final rinse with softened water can cause corrosion when processed in H2O2.

Any questions about preparation and assembly should be directed to:Case Medical, Inc at 19 Empire blvd, South Hackensack NJ 07606Phone: 1-(888)-227-CASE or (201)-313-1999. Fax: 201-373-9090To access our website, visit www.casemed.com

SteriTite Labelingfor Steam Sterilization using disposable filter

®

DEVICE DESCRIPTION: The SteriTite® container is a rigid, reusable, sealed medical sterilization packaging system. INTENDED USE: The SteriTite® container system is intended to be used for the sterilization of reusable surgicalinstruments and medical devices in health care facilities. MediTray products may be containerized or wrapped witha FDA cleared medical wrap. Please refer to the recommendations of your sterilizer manufacturer for specific processinginstructions as well as recommendations from your medical device manufacturer for material compatibility. LOAD: The contents must be placed within an instrument basket or tray. The load may be distributed in layers usingMediTray baskets or trays. When stacking trays, leave 1” of clearance in container. Case Medical validated maximum load of 35lbs including container and contents. AAMI recommends a maximum of 25lbs total weight.

PARAMETERS FOR USE:Prevacuum steam sterilization: Use vented or solid base container for pre-vacuum steam. Apply paper orpolypropylene disposable filter after each use. Use MediTray inserts in the container to secure instrumentation.Recommended for sterilization of medical devices including, blades and metal lumens of 2mm minimum diameter up to 435mm in length and porous lumens 3mm minimum diameter up to 400mm in length Recommendedexposure time: 4 minutes at 270°F. Minimum recommended dry time is 20 minutes. Pre-vacuum steam immediate use (flash) sterilization:Use vented or solid base container for pre-vacuum steam“IUSS” sterilization. IUSS sterilization is for immediate use only. Moisture may occur in IUSS cycles. Caution:Use a glove or towel when transporting hot items from the autoclave. Recommended exposure time: 4 min-utes at 270°F (132°C) with 0-3 min dry time. User may add additional dry time for a drier outcome. Disposable paperfilter SCF01 (7.5” diameter) and SCFM01 (10”X4”) are disposable medical device supplied nonsterile. Note: The user should contact their device manufacturer for appropriate (extended) sterilization cycle conditions. (ANSI/AAMI ST 79:2006 – Comprehensive guide to steam sterilization and sterility assurance in healthcare facilities). Gravity displacement steam:Use only perforated base containers for gravity displacement steam.Use MediTray basic trays in container. Select the appropriate exposure time based on load and size of container. Validation testing demonstrated kill in 15 to 25 minutes. Recommended minimum exposure time: 30 minutes at250°F. Minimum recommended dry time 30 minutes.Use of sealed containers may require additional exposure timein gravity displacement steam.Stackability of SteriTite® Containers in steam sterilization: Up to three (3) containers can be stacked and processed in the autoclave.WARNING: Prepare complex instruments according tothe instrument maker’s instructions. Use of nonabsorbent tray liners can cause condensate to pool. Do not use peelpouches within sealed containers, as they cannot be placed on their side for sterilization. Note: To reduce condensateformation, crack the autoclave door for 10 to 15 minutes to allow gradual cool down.EVENT RELATED STERILITY MAINTENENCE DATA: SteriTite containers are event related and maintainsterility during transport and multiple handling events, provided that the integrity of the seal is not broken. The associated tests consisted of testing samples after 30 to 90 days (real time) with handling events at a health care facility. SteriTite container for pre-vacuum flash was tested after a 24 hr period.VALIDATION TESTING: Case Medical subscribes to the overkill principle. SteriTite and MediTray products arevalidated in independent laboratories under fractional and half cycle conditions.

Contraindications: Dry heat and Formaldehyde sterilization.

Refer to the SteriTite® Instructions for Use and the ANSI/AAMI ST79: 2006/A1:2008* Comprehensive Guide toSteam Sterilization and Sterility Assurance in Health Care Facilities for sterilization guidelines. Review the sterilizer manufacturer’s operator manual for additional detail for specific sterilizaton systems.

Note: The SteriTite container with paper filter may be used for immediate use pre-vacuum steam sterilization cycles.